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. 2020 May 6;3(2):e155. doi: 10.1002/hsr2.155

Table 3.

Prevalence of genetic mutations in HCCs reported by different studies

Zhang et al 29 Ahn et al 31 Fujimoto et al 32 Guichard et al 33 Li et al 34 Huang et al 28 Schulze et al 30 TCGA cBioPortal 35 Current study 2020
Population China Korea Japan Not provided Not provided China Europe US Guatemala
N 49 231 300 125 139 110 243 366 18
TP53 82% 32% 28% 21% 28% 59% 25% 33% 44%
TP53 R249S 33%
AXIN1 20% 7% 5% 15% 20% 12% 2% 6%
CTNNB1 20% 23% 26% 33% 38% 17%
KIT 12%
SMARCA4 8% 6%
JAK3 8%
PBRM1 8%
GNAS 8% 6%
MED12 8%
RB1 8% 8% 6% 7% 11% 6%
RET 8%
ARID1A 6% 12% 17% 33% 12% 10% 17%
ARID2 6% 9% 6% 6% 4% 9% 28%
DNMT1 6%
DNMT3A 6% 6%
FLT3 6% 6%
ABL1 6%
FGFR2 6%
MAP3K1 6%
SETD2 6%
ARID1B 6%
CDKN2A 4% 6% 6% 7% 10% 8% 6%
ALB 4% 14% 12% 14% 6%
RPS6KA3 4% 6% 10% 9% 6%
CDKN1B 4%
MYC 4%
APC 2% 2% 17%
ATM 2% 44% 8% 11%
NFE2L2 6% 9% 7%
IRF2 5%
IL6ST 2% 4%
PIK3CA 2%
DMXL1 4%
KRAS 2% 3%
PTEN 4% 7%
CDKN1A 4%
FGFR3 11%
CASP8 0%